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IOSR Journal of Biotechnology and Biochemistry (IOSR-JBB)
ISSN: 2455-264X, Volume 6, Issue 1 (Jan. – Feb. 2020), PP 08-18
www.iosrjournals.org
DOI: 10.9790/264X-0601010818 www.iosrjournals.org 8 | Page
Evaluating the Potentials of Carica papaya seed as phytobiotic to
improve feed efficiency, growth performance and serum
biochemical prameters in broiler chickens
*Umar Muazu, Mohammed Aliyu-Paiko
*Department of Biochemistry, Ibrahim Badamasi Babangida University, Lapai, Nigeria
Corresponding Author: Umar Muazu
Abstract: Sixty day old chickens were randomly distributed into three treatments and fed diets mixed with 0,
0.5 and 1% papaya seed powder for the six weeks’ starter period. Feed consumption and growth performance
were monitored weekly. Lipid peroxidation was also assayed in the serum of the chicks from all treatments. At
the end of the experiment, results showed that feed efficiency and growth performance of broilers were not
significantly (p˃0.05) influenced by dietary treatments. The haematology parameters such as red blood cell,
haemoglobin, were significantly (p˂0.05) influenced by dietary inclusion of papaya seed powder. There were no
significant (p˃0.05) influence of papaya seed powder on serum biochemical parameters. Furthermore, lipid
peroxidation decreased significantly (p˂0.05) in treatments with papaya seed powder when compared to the
control. It may be concluded that feeding broiler chickens with diets mixed with papaya seed powder
significantly and positively reduced serum lipid peroxidation profile without negatively affecting feed efficiency,
growth performance and serum biochemical parameters.
Key words: Phytobiotic, Pawpaw seed powder, broiler, antioxidant, lipid peroxidation
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Date of Submission: 08-01-2020 Date of acceptance: 23-01-2020
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I. Introduction Poultry farming refers to the process of rearing domestic birds such as chickens, ducks turkeys, geese,
etc for the purpose of farming meat or eggs for food1. In Africa, agriculture and agro-industries account for over
30% of national incomes on average, as well as for the bulk of export revenues2. Nearly three-quarters of the
African population depend on agriculture to secure their livelihoods3 4
. As a result of high population growth in
Africa and the growing income, the demand for eggs and poultry meat has significantly increased in recent years
across large parts of the African continent5. Based on estimates by the United States Agency for International
Development, this trend is likely to continue over the next few years2. Therefore, the consumption of poultry
and eggs is projected to increase by about 200% between 2010 and 2020 in some countries in sub-Saharan
Africa, including Nigeria6 7
.
To increase production, use of feed additives in animal feeding began in the 1940s, to improve the
organoleptic characteristics of raw materials, fodders, and/or animal products, and to prevent diseases8 9
.
Additives are also used to improve production efficiency by decreasing the mortality rate and stimulating weight
gain10 11 12
. Different categories are common depending on their properties and functions13
.
Unfortunately, the risk posed by antibiotic growth promoters (AGPs) to create cross-resistance to
antibiotics used in human medicine and their presence in animal products, has led to their use to drop
significantly, this is as they are banned in some cases in the formulation of fodders and for use in general animal
husbandry14
. Some researchers however, suggested that the ban on these substances has caused increase in the
incidences of bacterial infections (i.e., diarrhea, coccidiosis and intestinal necrosis)14 11
. The prohibitions on
AGPs resulted in economic impact on the livestock industry because it led to increased production costs. The
American livestock industry demonstrated that the use of AGP in poultry production was associated with losses
for producers12 16
.
The restrictions on AGPs has stimulated interest in medicinal plants, which was revived in recent times
because of their efficacy in providing cost effective therapy to several diseases because of secondary metabolites
abundant in plants. Interestingly, Papaya (Carica papaya) is rich in polyphenols which makes them versatile
tools for the treatment of ailments in folklore medicine17
. Papaya is a common human fruit; available throughout
the year in the tropics. It is referred to as the "medicine tree" or "melon of health", and the major active
ingredients recorded include; carpine, chymopapain and papain, a bactericidal aglycone of glucotropaeolin,
benzyl isothiocyanate, a glycoside sinigrin, the enzyme myrosin, and carpasemine18
. This present study was
Evaluating the Potentials of Carica papaya seed as phytobiotic to improve feed …
DOI: 10.9790/264X-0601010818 www.iosrjournals.org 9 | Page
designed to investigate the effects of dried Carica papaya seed powder on growth performance, feed efficiency,
antioxidant enzyme activity, and serum biochemical parameters in broiler chickens.
II. Materials and Method Sixty day-old broiler starter birds were purchased from a commercial supplier in Minna, Niger state,
and transported to the research facility in ventilated paper cages. Day old broiler chicks were exposed to cross-
ventilation during the period of the study. Chicks were reared in cages of dimension 1.5 m x 1.5 m x 2.0 m;
length x breadth x height, that were previously cleaned and disinfected. Chicks were acclimated for 5 days.
During the acclimation, the chicks were fed commercial starter feed (23.62% Crude Protein, 14.7% Crude fat)
and water was supplied ad libitum under strict biosecurity control according to previously published protocol19
.
Study location: The feeding trial phase of this research study was carried out at the aquatic animal research
facility of biochemistry department Ibrahim Badamasi Babangida University, Lapai, Niger State.
Study design: Sixty day old chickens were randomly distributed into three treatments and fed commercial
starter feed (Chikun, Olam poultry feed mill, Kaduna, Nigeria) mixed with 0, 0.5 and 1% PSP for the six weeks’
starter period. Pre-weighed feed were provided to all treatments every morning to monitor feed intake while
drinking water were provided. Feed and water were offered to the birds in all the different treatments ad-libitum.
All birds were reared without vaccination. Chicks were reared under approximately natural photoperiod of 12/12
hours of light/dark cycles for period of six weeks and cages were cleaned at the end of every week.
Study duration: The experiment lasted for a period of 6 weeks of 7 days each.
Sample size: Sixty day-old broiler chicks’
Procedure methodology
Proximate composition analysis of experimental feeds and papaya seeds powder
Moisture content, crude fat, crude fiber, and crude protein (Microkjeldahl N x 6.25) were all determined
following standard Methods of the Association of Analytical Chemists20
.
Vitamin analysis
Vitamin analyses including vitamin C (ascorbic acid) and beta-carotene were determined in sample
(papaya seed powder) according to the method described by 2, 6-dichlorophenol indophenols method of Eleri
and Hughes21
whereas; Tocopherol was estimated in the sample by the Emmerie-Engel reaction as reported by
Rosenberg22
.
Calculations for feed efficiency and growth performance parameters
Various parameters were calculated by applying the appropriate formulae where necessary, using the following:
Chicks survival (%) = (total chicks’ survival/ total chicks stock) x 100
Weight gain %(WG %) = [(Wf - Wi)/Wi] x 100
Specific growth rate (SGR %) = [(ln Wf - ln Wi)/T] x 100
Feed intake (FI) = total feed intake/number of live chicks
Feed conversion ratio (FCR) = wet weight gain (g)/feed intake (g)
Where Wf refers to the mean final weight, Wi is the mean initial weight and T is the feeding trial period in days.
Determination of haematological parameters Haematological components including red blood cells (RBC), haemoglobin (HGB), Mean cell volume
(MCV), hematocrit (HCT%), Platelet number (PLT), white blood cells (WBC), lyphocytes (LYM), Mean cell
haemoglobin, (MCH), Mean cell haemoglobin concentration (MCHC), Mean platelet volume (MPV), were
determined using the automated haematologic analyzer (ABACUS 3CT, Diatron, USA), employing the methods
described by Dacie and Lewis23
.
Determination of Serum biochemical analysis
Chicks serum biochemical analysis such as AST, ALT, ALP, bilirubin, albumin, creatinine, proteins,
potassium, chloride, sodium and urea were determined spectrophotometrically following the manufacturer’s
instructions of AGAPPE diagnostics, Cham, Switzerland while Lipid peroxidation was assayed according to the
method described by Health and Parker24
.
Determination of activities of antioxidant enzymes
Antioxidant enzymes including superoxide dismutase (SOD) and catalase (CAT) were determined
spectrophotometrically from chicks’ serum according to the method described by Yusuf, where lipid
peroxidation was assayed according to the method described by Health and Parker24
.
Evaluating the Potentials of Carica papaya seed as phytobiotic to improve feed …
DOI: 10.9790/264X-0601010818 www.iosrjournals.org 10 | Page
Statistical analysis
Data obtained were subjected to one-way analysis of variance (ANOVA) and the means were
compared using Turkeys test. Statistical significance was set at P ˂ 0.05. Statistical analyses were performed
using SPSS software Version 20.0. Data for all determinations are presented as mean ± SEM of three replicates.
III. Results No chickens died during the experiment, as 100 % of the chickens from all treatments survived. Results
for proximate composition analysis of PSP and all dietary treatments are shown in Table 1. From the Table, it is
observed that PSP is a good source of fat, protein and fibre. The moisture content of PSP was low. The result
also showed moderate value of ash content that suggests papaya would provide essentials minerals.
Furthermore, PSP also contains antioxidant enzymes such as vitamin C, E and β-carotene. Inclusion of PSP up
to 1 % did not significantly (P ˃ 0.05) modify the nutrient composition of all dietary treatments compared to the
control.
Table 1: Proximate composition of experimental feeds and Carica papaya seed powder
Treatments
Parameters PSP 0 % PSP 0.50 % PSP 1 % PSP
MC % 6.81±0.00 8.44±0.01a 7.56±0.01a 7.66±0.01a
CF % 30.80±0.03 4.90±0.01a 5.90±0.01a 6.50±0.01a
ASH % 2.09±0.00 4.30±0.01a 5.95±0.01a 7.10±0.01a
FAT % 28.19±0.00 14.70±0.01a 12.0±0.01a 13.67±0.01a
CP % 26.25±7.99 23.62±0.01a 27.12±0.01a 32.37±0.01a
CHO % 5.86±0.01 44.04±0.01a 34.97±0.01a 39.20±0.01a
Vit C (mg/100g 0.85±0.02 Vit E (µg/100g 2.00±0.33
β-carotene (mg/100g) 0.40±0.03
Data are expressed as mean ± SEM (n = 20).
Mean ± SEM followed by different superscript letter within a row are significantly different (P <0.05).
MC, Moisture content; CF, Crude fibre; CP, Crude protein; CHO, Carbohydrate (Nitrogen free extract).
Table 2 showed the results for feed efficiency and growth performance of broiler chickens fed graded
level of PSP for starter period. The data indicated that weight gain increased with increasing level of PSP in the
diet from 0.5% to 1.0 %. Generally, better feed conversion ratio values were obtained in all treatments, but
getting poor with increase of dietary PSP up to 1 %. Chicks fed diet containing 0.5 % PSP had better feed
conversion ratio compared to the control. Feed intake was significantly (P ˂ 0.05) the highest in 1% PSP.
Table 2: Feed efficiency and growth performance of broiler chickens fed graded level of C. papaya seed powder
for 6 weeks starter period.
Dietary treatments
Parameters 0 % PSP 0.50 % PSP 1 % PSP
Growth performance
Mean initial weight (g) 69.20±2.44a 66.55±1.92a 68.25±1.48a
Mean final weight (g) 2001.7±57.81a 2079.75±60.46a 2175.67±82.79b Specific growth rate (%) 8.00±0.24 8.19±0.04 7.88±0.05
Weight gain (g) 1932.50±0.12a 2013.25±0.19a 2085.42±0.16a
Av. Daily weight gain (g) 46.00±0.31 47.93±0.04 49.64±0.21 Feed efficiency
Feed intake (g) 3498.75±0.25a 3462.75±0.25a 4084.28±0.09b
Feed conversion ratio 1.81±0.00 1.72±0.01 1.96±0.02
Data are expressed as mean ± SEM (n = 20).
Mean ± SEM followed by different letter within a row are significantly different (P <0.05).
Haematology parameters measured in broiler chickens fed graded level of PSP diets are as shown in
Evaluating the Potentials of Carica papaya seed as phytobiotic to improve feed …
DOI: 10.9790/264X-0601010818 www.iosrjournals.org 11 | Page
Table 3. From the Table, the haematology parameters such as MCV, HCT% and PLT did not significantly (P ˃
0.05) differ across all the treatments. RBC and HGB values recorded were higher (P ˂ 0.05) in 0 % free PSP
diet group compared to 0.5 % PSP supplemented group and it became lower with the increased in PSP up to 1 %
PSP. Chicks fed 0.5 % PSP had higher but not significant (P ˃ 0.05) MCV value when compared to control.
Furthermore, chicks fed diet containing 1 % PSP recorded the least MCV value. HCT which is the percent of
whole blood made up of red blood cell showed a dose dependent effect of PSP supplementation.
Table 3: Haematology parameters of broiler chickens fed graded level of c. papaya seed powder for 6 weeks
starter period.
Treatments
Parameters 0 % PSP 0.5 % PSP 1 % PSP
RBC (× 106mm-3) 8.49±2.58a 6.37±0.40b 3.83±0.63c
HGB (g/dl) 14.63±0.20a 13.93±0.22ab 11.87±3.37b
MCV (m3) 126.67±0.33a 127.67±1.33a 125.67±1.20a
HCT (%) 28.35±0.21a 27.61±0.73a 23.51±6.89a
PLT (mcL) 3.00±0.57a 2.33±0.88a 3.00±2.52a
Data are expressed as mean ± SEM (n = 3).
Mean ± SEM followed by different letter within a row are significantly different (P <0.05).
RBC, Red blood cell number; HGB, Haemoglobin; MCV, Mean cell volume; HCT, Haematocrit; PLT, Platelet
number.
The result of blood parameters of broiler chickens fed graded level of PSP diets are as shown in Table
4. Blood parameters such as WBC, LYM, MCH, MCHC and MPV did not significantly (P ˃ 0.05) differ across
all the treatments. The result of MCH, which is the average amount of HGB in each RBC measured, followed
the same pattern as MCV.
Table 4: Blood parameters of broiler chickens fed graded level of C. papaya seed powder for 6 weeks starter
period.
Treatments
Parameters 0% PSP 0.5 % PSP 1% PSP
WBC (× 106mm-3) 89.20±0.91a 74.34±12.53a 42.02±12.08a
LYM (%) 62.37±5.62a 54.07±12.94a 30.75±9.61a
MCH (pg) 65.20±0.50a 64.53±0.92a 63.87±1.30a
MCHC (g/dL) 51.50±0.45a 50.60±0.80a 50.83±0.90a
MPV (fL) 9.87±1.78a 10.40±1.16a 5.80±2.99a
Data are expressed as mean ± SEM (n = 3).
Mean ± SEM followed by different letter within a row are significantly different (P <0.05).
WBC, White blood cell number; LYM, Lymphocytes; MCH, Mean cell haemoglobin; MCHC, Mean cell
haemoglobin concentration; MPV, Mean platelet volume.
Results for hepatic and renal function biomarkers of broiler chickens fed graded level of PSP for 6
weeks starter period are shown in Table 5. The result showed no significant difference (P ˃ 0.05) across all the
treatments, of the biomarkers monitored. Although, values of AST and ALT obtained in broiler chicks fed PSP
containing diet were lower when compared to the control diet (0 % PSP) which, however, still falls within the
normal range in chickens which ranged from 1-37 µL25
.
Evaluating the Potentials of Carica papaya seed as phytobiotic to improve feed …
DOI: 10.9790/264X-0601010818 www.iosrjournals.org 12 | Page
Table 5: Hepatic and Renal function biomarker of broiler chickens fed graded level of C. papaya seed powder
for 6 weeks starter period.
Treatments
Parameters 0% PSP 0.50% PSP 1% PSP
AST (µL) 16.80±1.25a 16.20±0.46a 15.17±1.89a
ALT (µL) 18.90±0.76a 17.93±2.72a 17.97±0.59a
ALP (µL) 25.97±1.86a 27.23±1.88a 28.87±0.82a
Bil-total (mg/dl) 1.93±0.14a 1.87±0.23a 1.47±0.18a
Bil-direct (mg/dl) 1.43±0.07a 1.67±0.23a 1.43±0.03a
Albumin (µl) 1.63±0.07a 1.43±0.07a 1.63±0.03a
Data are expressed as mean ± SEM (n = 3).
Mean ± SEM followed by different letter within a row are significantly different (P <0.05).
AST, Aspertate aminotransferase; ALT, Alanin aminotranferase; ALP, Alkline phosphate.
The result of serum metabolic parameters of broiler chickens fed graded level of PSP diets are as
shown in Table 6. The result of serum metabolic parameters; total protein, creatinine, urea, potassium, chloride
and sodium did not significantly (P ˃ 0.05) differ across all the treatments. Creatinine values of broiler chickens
fed PSP containing diet were numerically not significant (P ˃ 0.05) different compared to the control.
Table 6: Serum metabolic parameters of broiler chickens fed graded level of C. papaya seed powder for 6
weeks starter period.
Treatments
Parameters 0 % PSP 0.5 % PSP 1 % PSP
Total protein (g/dl) 1.70±0.06a 1.67±0.09a 2.00±0.15a
Creatinine (mg/dl) 1.40±0.11a 1.30±0.06a 1.27±0.03a
Urea (mg/dl) 46.50±0.26a 46.57±0.26a 47.63±0.43a
Potassium (mmol/l) 3.43±0.22a 3.90±0.21a 3.47±0.13a
Chloride (meq/l) 53.23±1.57a 61.33±3.56a 95.43±17.09a
Sodium (meq/l) 114.17±1.82a 148.57±4.37a 127.07±5.47a
Data are expressed as mean ± SEM (n = 3).
Mean ± SEM followed by different letter within a row are significantly different (P <0.05).
Serum antioxidant enzymes (SOD and catalase) activities and LPO data for broiler chickens fed graded
level of PSP diets are as shown in Table 7. The activities of superoxide dismutase and catalase as antioxidant
enzymes were significantly (P<0.05) elevated in treatment with PSP when compared to the control (0 % PSP).
The result of antioxidant enzyme activity (SOD and CAT) showed a significant (P˂0.05) increase in 1 % PSP
compared with the control, but 0.5 % PSP had no significant increase compared with the control. However, lipid
peroxidation profile decreased significantly (P ˂ 0.05) in treatment with PSP when compared to the control, and
peroxidation decreased with more PSP in the diet.
Evaluating the Potentials of Carica papaya seed as phytobiotic to improve feed …
DOI: 10.9790/264X-0601010818 www.iosrjournals.org 13 | Page
Table 7: Serum antioxidant enzyme activity of broiler chickens fed graded level of C. papaya seed powder for 6
weeks starter period.
Treatments
Parameters 0 % PSP 0.5 % PSP 1 % PSP
SOD (µ/l) 2.60±0.23a 3.03±0.03ab 4.87±0.9b
CAT (µ/l) 2.66±0.41a 3.48±0.08ab 4.14±0.08b
LPO (nmol/ml) 5.98±1.33a 2.86±0.04b 1.77±0.21b
Data are expressed as mean ± SEM (n = 3).
Mean ± SEM followed by different letter within a row are significantly different (P<0.05).
SOD, Superoxide dismutase; CAT, Catalase; LPO, Lipid peroxidation assay.
IV. Discussion No chickens died during the experiment, as all (100 %) of the chickens from all treatments survived.
The survival of all chickens from all treatment is an indication that PSP may not contain any toxic substances.
No vaccines or AGPs were used in the study.
The crude protein content for PSP was noted to be high indicating that it is a very good source of
protein (Table 1). Protein is an essential component of diet needed for the survival of both animal and human of
which basic function is to supply adequate amount required26
. Protein represent key nutrient for muscle and
bone health, and thereby function in the prevention of osteoporosis in chickens27
. The protein content of PSP
noted in the present study was similar to that reported by Makanjuola28
and Maisarah, et al.29
.
PSP was also noticed to be a good source of fiber. According to Eromosele30
fibre helps in the
maintenance of animal health and has been known to reduce cholesterol level in the body. A high fibre food
expands the internal wall of the colon, causing the passage of waste, thus making it an effective anti-
constipation. Fibre also reduces the risk of various cancers, bowel diseases and improves general health and
well-being of animals. The crude fibre content of PSP recorded in the present study was similar to that reported
by Adebisi, and Olagunju31
.
Fat content of PSP was recorded to be high indicating that PSP is a good source of oil which can serve
as energy source. According to Wood, et al.32
dietary intake of fat (unsaturated fatty acids) reduces the risk of
cardiovascular disease and possibly the incidence of some cancers, asthma and diabetes in chickens. The fat
content of PSP in the present study was similar to that reported by Makanjuola28
.
The moisture content of PSP was low. Low moisture contents generally are an indication of high shelf
life especially for foods that are properly packaged against external condition28
. Similar results were earlier
reported by Chan-Prove et al.33
.
Furthermore, PSP also contains antioxidant enzymes such as vitamin C, E and β-carotene. Vitamin C
content of PSP in this study was recorded to be low compared to previous literature29
. Souza et al.34
reported
higher ascorbic acid content which was varied in two different species of papaya. Papaya is a source of vitamin
C with amounts varying between the maturation stages 35 36
. Variation in vitamin C content was also reported
among papaya varieties37
. Vitamin C is an important antioxidant in aqueous phase, capable of scavenging
oxygen derived free radicals38
. Wall37
suggested that papayas supply good quality of vitamins C and A. Papaya
ranks first among 13-17 fresh fruits for vitamin C content39
.
PSP was also noted to contain Vitamin E in a moderate quantity. Vitamin E is one of the most
important lipid-soluble primary defense antioxidants40 41
. Vitamin E scavenges peroxyl radical intermediates in
lipid peroxidation and responsible for protecting Poly Unsaturated Fatty Acid (PUFA) present in cell membrane
and low density lipoprotein (LDL), against lipid peroxidation42
. However Rojas and Campos43
reported Vitamin
E content for ripe papaya in moderate quantity and this was quite similar to that in the present study.
From the result of this study, beta-carotene was also noticed to be present in PSP. Beta-carotene has
antioxidant properties that can help neutralize free radicals (reactive oxygen molecules) that potentially damage
lipids in cell membranes and genetic material. This may lead to the development of cardiovascular disease and
cancer44
. Mean beta carotene content observed in this study was higher than previously reported by Souza et
al.34
. The differences in the beta carotene content observed could be attributed to methods of analysis that have
been shown to contribute to variations in reported beta-carotene contents45
.
Inclusion of PSP up to 1 % did not significantly alter nutrient composition of all dietary treatments
compared to the control. The result obtained from this study is thus likely due to the quantity added. According
to Windisch et al.46
supplementation levels of products to poultry diets vary between 0.1 and 40 g/kg for dried
products and plant extracts. In addition, phytobiotics (PSP) are substance added to feed to improve the safety,
flavor, taste, and other qualities of the feed47 48
and do not add significantly to the main nutrients of the feed.
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DOI: 10.9790/264X-0601010818 www.iosrjournals.org 14 | Page
Weight gain in poultry remained (P ˃ 0.05) with increasing level of PSP in the diet from 0.5% to 1.0 %
(Table 2). Usually, increase weight gain by broiler chicks fed additive containing diet observed in this study
could be attributed to the fact that herbal plants provide compounds that enhance digestion and absorption of
nutrients in diets, leading to improved growth of chicks49
. The result of this study was not in concordance with
that of Mohamed et al.50
, and Arshad et al.51
who reported significant (P < 0.05) increase in live body weight of
broiler chicks fed ginger-supplemented diet.
Generally, better feed conversion ratio values were obtained in chicks fed all treatments, but getting
poor with increase of dietary PSP up to 1 % PP. Chicks fed diet containing 0.5 % PP had better feed conversion
ratio. Better feed conversion ratio of the broiler chicks fed diet containing PSP additive could be attributed to the
antibacterial properties of these additive, which may have resulted in better absorption of the nutrients present in
the gut and finely leading to improvement in feed conversion ratio of the treatments group52
.
The broiler chicks fed PSP diets showed better feed intake compared to the control (Table 2). Feed
intake was significantly (P ˂ 0.05) the highest in 1% PSP. Feed intake of broilers in this study showed that
feeding PSP resulted in dose-related effect on palatability53 54
. Better feed intake of broiler chicks fed PSP diets
could be attributed to an improvement in the oganoleptic characteristics of feed as a result of adding PSP.
Arshad51
, and Herawati55
, reported similar results in feed intake when broiler chicks were fed diet containing
ginger powder as phytobiotics additives.
Blood acts as a pathological reflector of the status of animals exposed to xenobiotics and other extreme
conditions56
. As reported by Isaac et al.57
animals with healthy blood composition are likely to show good
performance. Laboratory tests on the blood are vital tools that help detect any deviation from normal health
status in animals58
. The examination of blood gives the opportunity to investigate the presence of several
metabolites and other constituents in the body of animals and also play vital roles in the physiological,
nutritional and pathological status of an organism59 60
. According to Afolabi et al.61
, changes in haematological
parameters are often used to determine status of the body and stresses due to environmental, nutritional and/or
pathological factors.
Haematology parameters such as MCV, HCT% and PLT did not significantly (P ˃ 0.05) differ across
all the treatments (Table 4.5). Generally, inadequate intake of energy and protein adversely affect RBC, HGB,
MCV and HCT or packed cell volume (PCV) concentration which indicates anaemia62 63
. RBC and HGB values
recorded were higher (P ˃ 0.05) in the PSP- free diet group compared to 0.5 % PSP supplemented group and it
became lower with the increase in PSP up to 1 % PSP. The increase observed in broiler chicken fed 0 % PSP
diet might be due to the greater oxygen demand for activity64
. Moreover, Palomeque et al.65
reported that
increased haemoglobin content per unit of volume of blood may be a reflection of decreased volume of blood
per unit body weight.
The normal values of HCT obtained in the present study indicated that the PSP added to chicken diet
increased the availability of protein, energy and the degradation of anti-nutritional factors. This according to
Cary, et al.66
could consequently improve broiler performance. This confirmed that haematological traits,
especially HCT and HGB were correlated with the nutritional status of the animal67
and agreed with Oyawoye,
and Ogunkunle68
, who stated that PCV is an index of toxicity in the blood and high levels usually suggest the
presence of toxic factors which has adverse effect on blood formation.
Blood parameters such as WBC, LYM, MCH, MCHC and MPV did not significantly (P ˃ 0.05) differ
across all the treatments (Table 4.6). The normal values of WBC, platelets, and MCHC recorded for broiler
chicks fed PSP diet may be indication that the bone marrows of the broiler chickens were properly functional
and also revealed the absence of macrocytic and hypochronic anaemia69
.
Normal value of WBC recorded for broiler chickens fed PSP diet is probable due to the ability of PSP
to cause destruction or impaired production of white blood cells, probably by affecting the production of
regulatory factors involved in haematopoesis70
. However, PSP has been shown to have antioxidant properties
which could equally suppress production of white blood cells71
.
The result of MCH, which is the average amount of HGB in each RBC measured, followed the same
pattern as MCV. The MCV and MCH values obtained in broiler chickens fed PSP diet and PSP free diet in this
study fall within the normal range of 90 to 140 fl and 16 to 65pg72 73
. The result of this study is in line with that
reported by Tuleun et al.74
in broiler chickens and Adenkola et al.75
in rabbits that nutrient is an important factor
in haemopoesis. .
Hepatic and renal function biomarkers of broiler chickens fed graded level of PSP for 6 weeks starter
period showed AST, ALT and ALP values not significantly varied (P ˃ 0.05) across all the treatments (Table
4.7). Notably, the values of AST and ALT obtained in broiler chicks fed PSP containing diet were lower when
compared to the control diet (0 % PSP) which, however, still falls within the normal range in chickens; from 1-
37 µL25
. This likely influenced the ability of birds to withstand the effect of anti-nutritional factors (if any)
which could cause liver damage76
. This was similar with the findings recorded by Ekpenyong and Biobaku77
,
Evaluating the Potentials of Carica papaya seed as phytobiotic to improve feed …
DOI: 10.9790/264X-0601010818 www.iosrjournals.org 15 | Page
who stated that the values of AST and ALT are normally low in blood but becomes high when there is
occurrence of liver damage by toxic substances.
Similar values of AST and ALT that were not significantly varied (p˃0.05) in this study for the control
(0% PP) relative to treatments are indicative of normal liver and kidney functions78 79
that did not worsen by
addition of more PSP.
The result of the serum metabolic parameters; serum albumin, creatinine, urea and total protein of
treatments (0.5% PP and 1% PP) (Table 4.8) were similar with that for the control (0% PP). High urea and
creatinine values are a measure of especially muscle amino acid degradation80
, and early pointer to depressed
liver and kidney functions81
.
Creatinine values of broiler chickens fed PSP containing diet were numerically lower but not
significant (P ˃ 0.05) compared to the control. Elevated creatinine value in broiler chickens fed PSP-free diet
may suggest depletion of tissue creatinine phosphate and this may adversely affect the muscle mass82 83
. This
could imply that there was slightly better protein metabolism and utilization in the treatment group than the
control. Therefore, PSP can be used with confidence in broiler diet to provide adequate nutrition.
The result of the activities of Superoxide Dismutase and Catalase as antioxidant enzymes were
significantly (P<0.05) elevated in treatment with PSP when compared to the control (Table 4.9). The values of
SOD and CAT increased significantly (P˂0.05) with increasing levels of PSP. Oxidative stress is the potential
mechanism that overwhelms the primary antioxidant defense of the body. Antioxidants function by suppressing
the formation of reactive oxygen species (ROS) and reactive nitrogen species (RNS), affecting enzyme
activities29
. SOD is one of the crucial antioxidant defenses of the body, and only enzyme family with activity
against superoxide radicals. SOD enzymes are present in almost all aerobic cells and in extracellular fluids84
.
Catalases are enzymes that catalyses the conversion of hydrogen peroxide to water (H2O) and oxygen
(O2), using either an iron or manganese cofactor85 86
. This protein is localized to peroxisomes in most eukaryotic
cells87
. Therefore, increased values recorded as the dietary level of additive was increased from 0.5% PP to 1%
PP could be attributed to antioxidant effect of papaya seeds which stimulated the activities of both superoxide
dismutase and catalase enzymes.
Conversely, lipid peroxidation profile decreased significantly (p˂0.05) in treatments with PSP when
compared to the control (Table 4.9). Lipid peroxidation is the oxidative degradation of lipids. It is the process in
which free radicals steals electrons from the lipid in cell membranes, resulting in cell damage88
. In this study,
lipid perodixidation values tended to decrease as the dietary level of PSP was increased from 0.5% PP to 1% PP.
This may be attributed to the antioxidant effects of PSP which are capable of neutralizing reactive oxygen
species before lipid peroxidation is initiated89
. Similar result was reported by Antache, et al.90
who showed that
the supplementation of Nile tilapia feed with rosemary, sea buckthorn and ginger in 1% concentration led to
reduction in malondialdehyde concentration, and increased total antioxidant capacity from various tissues.
V. Conclusion From the results of this experimentation, feeding broiler chickens with diets mixed with PSP
significantly and positively reduced serum lipid peroxidation profile without negatively affecting feed
efficiency, growth performance and serum biochemical parameters. Therefore, PSP could be supplemented in
feed as phytobitic additives because it has potentials as antioxidant when supplemented in the diets of broiler
chickens.
References [1]. Beutler, A. 2007. Introduction to Poultry Production in Saskatchewan, University of Saskatchewan, Saskatoon, Saskatchewan, S7N
5A8. Accessed: November 18, 2009 [2]. Heise, H., Crisanb, A. and Theuvsenc, L. (2015). The Poultry Market in Nigeria: Market Structures and Potential for Investment in
the Market International Food and Agribusiness Management Review Volume 18 Special Issue A
[3]. Connolly, A. J. 2014. A Glimpse into the Future: A Lens through Which to Consider ‘Africa’s Rising’. International Food and Agribusiness Management Review 17(Special Issue B): 9-18.
[4]. Oram, J. (2012). A New Direction for Agriculture. Greenpeace.
http://www.greenpeace.org/international/Global/international/publications/RioPlus20/New-Direction-for-Agriculture.pdf [accessed August 26, 2014].
[5]. World Health Organization. 2010. World Health Statistics.
[6]. United States Department of Agriculture (USDA). 2013. International Egg and Poultry Report. [7]. Obi, C.I. 2003. Game production: An alternative beef cattle production in Southern Nigeria. Academic Forum 4:36-40.
[8]. US Food Administration. Guidance for industry #209: the Judicious use of Medically important Antimicrobial Drugs in Food-
Producing Animals. 2012. Available at: http//www.fda.gov/downloads/AnimalVeterinary/ GuidanceCompliance Enforcement/ GaidanceforIndustry/UCM216936.pdf. 19 August 2013
[9]. Sapkota, A.R., Lefferts, L.Y., McKenzie, S. and Walker, P. (2007). What do we feed to food-production animals? A review of
animal feed ingredients and their potential impacts on human health. Environ Health Perspect. 115:663-670. [10]. Upadhayay, U. P., P. D. D. and Vishwa, P. C. V. (2014).Growth Promoters and Novel Feed AdditivesImproving Poultry Production
and Health,Bioactive Principles and BeneficialApplications: The Trends and Advances—AReview. Int. J. Pharm.10(3), 129-159.
Evaluating the Potentials of Carica papaya seed as phytobiotic to improve feed …
DOI: 10.9790/264X-0601010818 www.iosrjournals.org 16 | Page
[11]. Castanon, J. I. R. (2007) History of the Use of Antibiotic as Growth Promotersin European Poultry Feeds. Poultry Science
86(11):2466–2471doi:10.3382/ps.2007-00249
[12]. Dibner, J. J., and J. D. Richards. 2005. Antibiotic growth promoters in agriculture: History and mode of action. Poult. Sci. 84:634–643.
[13]. Marroquin-Cardona, A., Deng, Y.. Taylor, J. F., Hallmark, C. T.., Johnson, N. M. and Phillips, T. D. (2010). In vitro and in vivo
characterization of mycotoxin-binding additives used for animal feeds in Mexico. Food Addit. Contam.26(5),733-743. [14]. Gaucher, M. L., Quessy, S. Letellier, A. Arsenault, J. and Boulianne, M. (2015). Impact of a drug-freeprogram on broiler chicken
growthperformances, gut health, Clostridiumperfringens and Campylobacter jejunioccurrences at the farm level. Poult. Sci.
94(8),1791-1801. [15]. Allen, P.C., Fetterer, R.H. etal., (2013). Recent advances in biology and immunology of Eimeriaspecies and in diagnosis and control
of infection with coccidian parasites of poultry. Clin. Microbiol. Rev. 15:58–65.
[16]. Graham, J. P., Boland, J. J. and Silbergeld, E. (2007).Growth promoting antibiotics in food animalproduction: an economic analysis. Public HealthRep. 122(1), 79.
[17]. Wang, J., Wu, F. A., Zhao, H., Liu, L. and Wu, Q. S. (2008). Isolation of flavonoids from mulberry (Morus alba L.) leaves with
macroporous resins. African Journal of Biotechnology 7: 2147-2155. [18]. JackWheeler, M.N. (2003). Healthmate Papaya. http://www.Papaya_aspx.htm.
[19]. Molla et al. (2012). Patients’ perceptions of podoconiosis causes, prevention and consequences in East and West Gojam, Northern
Ethiopia. BMC Public Health 12:828. [20]. AOAC, (2002). Association of Official Analytical Chemists. Official Method of Analysis. 17th Edn. Gaithersburg, USA.
[21]. Eleri, J. and Hughes, R.E. (1983). Foliar ascorbic acid in some angiosperms. Phytochemistry Volume 22, Issue 11, Pages 2493-
2499. [22]. Rosenberg, E. B. (1992). The adoption life cycle: The children and their families through the years. New York, NY, US: Free Press.
[23]. Dacie, J.V. and Lewis, S.M. (1991). Practical Haematology. 7th Edition, Churchil Livingstone, Edinburgh, 54-79.
[24]. Health, R. L. and Parker, L. (1968). Photoperoxidation in isolated chloroplast I. Kinetics and stoichiometry of fatty acid peroxidation. Archives of Biochemistry and Biophysics, 125, 189-198.
[25]. Ker, G. R., E. Lee, S. Lan, M. K. M. Larmor, R. J. Randell, E. and Forhoter, R. (1982) Relationship between dieting and
biochemical measures of nutritional status. Am. J. Clin. Nutr., 35: 294-308. [26]. Pugalenthi, M., Vadived, V., Gurumoorthi, P. and Janardhanan (2004). Comparative nutritional evaluation of little known legumes;
Tamarindusindica, Erthrina indica and Sesbaniab ispinosa. Tropical, Sub-tropical Agro-ecosystem 4:107-123.
[27]. Bonjour, J. P. (2011). Protein intake and bone health. Int J Vitam Nutr Res 81:134-142. [28]. Makanjuola, O. M. and Makanjuola, J. O. (2018). Proximate and selected mineral composition of ripe pawpaw (Carica papaya)
seeds and skin. Journal of Scientific and Innovative Research 7(3): 75-77
[29]. Maisarah, A.M., Asmah, R. and Fauziah, O. (2014) Proximate Analysis, Antioxidant and Antiproliferative Activities of Different Parts of Carica Papaya. J Nutr Food Sci 4: 267.
[30]. Eromosele, I.C. and Eromosele, C.O. (1993). Studies on the chemical composition and physiochemical properties of seeds of some
wild plant. (Netherland). Plant Food for Human Nutrition. 43:251-258. [31]. Adebisi, G.A. and Olagunju, E.O. (2011). Nutrition of the seed of Fluted Pumpkin. (Telfairia occidentalis). Journal of New Trend in
Science and Technology Application 1(1):7-18.
[32]. Wood, J.D., Richardson, R.I., Nute, G.R. Fisher, A.V., Campo, M.M., Kasapidou, E., Sheard, P.R. and Enser, M. (2003). Effect of
fatty acids on meat quality; a review. Meat Sci. 66: 21-32.
[33]. Chan-Prove, P., Rose, P.O., Hane, P., Macleod, N., Kernot, I., Evan, D. et al. (2010). Agriclink series; Your growing guide to better farming. Pawpaw information kit. Queensland Horticulture Institute and Department of Primary Industries Qld, Nambour.
[34]. Souza Jr. MT, Venturoli MF, Coelho MCF, Rech Filho EL (2001) Analysis of marker gene/selective agent systems alternatives to
positive selection of transgenic papaya (Carica papaya L.) somatic embryos. Revista Brasileira de Fisiologia Vegetal 13: 365-372. [35]. Bari, L., Hassan, P., Absar, N., Haque, M.E., Khuda, M.I.I.E., Pervin, M.M., Khatu, S. and Hossain, M.I. (2006). Nutritional
analysis of two local varieties of papaya (Carica papaya L.) at different maturation stages. Pakistan Journal of Biological Sciences
9(1):137-140. [36]. Hernández, H., et al. (2006) Subunit architecture of multimeric complexes isolated directly from cells. EMBO Rep 7(6):605-10
[37]. Wall, M.M. (2006) Ascorbic acid, vitamin A, and mineral composition of banana (Musasp.) and papaya (Carica papaya) cultivars
grown in Hawaii. J Food Compos Anal 19: 434-445. [38]. Gebbhardt SE, Thomas RG (2002) Nutritive value of foods. U.S. Department of Agriculture, Home and Garden Bulletin 72
[39]. Abdalla, A.E. (2009). The role of antioxidant (Vitamin E) in the control of lead pollution and enhancement of growth within Nile
tilapia (Oreochromis niloticus). International J. Applied Res. Veterinary Medical, 3:97-101. [40]. Handan, M.K. Suleyman, M. and Yeter, D. (2007). Vitamin status in yearling rams with growth failure. Turkey J. Veterinary
Animal Sci 31:407-409
[41]. Vivek, K.G. and Surendra, K.S. (2006). Plants as natural antioxidants. Natural. Production. Radia., 5: 326-334. [42]. Monge-Rojasa, R. and Campos, H. (2011) Tocopherol and carotenoid content of foods commonly consumed in Costa Rica. JFood
Comp Anal 24: 202-216.
[43]. Pavia, S.A. and Russell, R.M. (1999) Beta-carotene and other carotenoids as antioxidants. J. American Coll. Nutrition., 18: 426-433.
[44]. Rodriguez-Amaya, D. B., Kimura, M. and Amaya-Farfan, J. (2008). Brazilian sources of carotenoids. (Fontes brasileiras de
carotenoids). Brasília, DF: Ministério do Meio Ambiente. [45]. Windisch W., Rohrer E., Schedle K., 2009. Phytogenic feed additives to young piglets and poultry: mechanisms and application. In:
T. Steiner (Editor). Phytogenics in Animal Nutrition. Nottingham University Press, Nottingham, ISBN 978-1-904761-71-6
[46]. FDA, (2018). Food ingredients and packaging terms. Retrieved 9 September 2018. [47]. Erich, L. and Gert-Wolfhard V.R.L. (2002). "Foods, 3. Food Additives" in Ullmann's EncyclopediaofIndustrial Chemistry,,
WileyVCH, Weinheim. doi:10.1002/14356007.a11_561
[48]. Safa, E., Mohamed, K.A. and Mukhtar, M.A. (2014) Effect of using Garlic powder as natural feed additive on performance and carcass quality of Broiler chicks. Assiut Vet Med J 2014 60: 141: 45-53.
[49]. Mohamed, A.B., Mohammed, A.M. and Ali-Jalil, Q. (2012) Effect of ginger (Zingiber officinale) on performance and blood serum
parameters of broiler. Int. J. Poult. Sci. 11(2):143–146. [50]. Arshad M, Kakar A.H, Durrani F.R, Akhtar A, Sanaullah S, Niamatullah M. (2012). Economical and immunological impact of
ginger extract on broiler chicks. Pak. J. Sci.;64(1):46–48.
Evaluating the Potentials of Carica papaya seed as phytobiotic to improve feed …
DOI: 10.9790/264X-0601010818 www.iosrjournals.org 17 | Page
[51]. Khatun, S., Mostofa, M., Alom, F., Uddin, J., Alam, M.R. and Moitry, N.F. (2013). Efficacy of tulsi and papaya leaves extract in
broiler production. Bangladesh Journal of Veterinary Medicine 11: 1-5.
[52]. Jugl-Chizzola, M., Ungerhofer, E., Gabler, C., Hangmuller, W., Chiz-zola, R., Zitterl-Egleer, K. and Franz, C. (2006). Testing of the palatability of Thymus vulgaris L. and Origanum vulgaris L. as flavouring feed additive for weaner pigs on basis of a choice
experiment. Beri Munch Tierarztl Wochenschr 119: 238-243
[53]. Schone, F., Vetter, A., Hartung, H., Bergmann, H., Biertumpfel, A., Richter, G., Muller, S. and Breitchuh, G. (2006). Effect of essential oil from fennel (Foeniculi aetheroleum) and caraway (Carvi aetheroleum) in pigs. J. Anim Physiol Anim Nutr (Berl) 90:
500-510.
[54]. Herawati, Marjuki (2011). The effect of feeding red ginger (Zingiber officinale rose) as phytobiotic on broiler slaughter weight and meat quality. Int. J. Poult. Sci. 10(12):983–985. [Google Scholar]
[55]. Olafedehan, C. O., Obun, A. M., Yusuf, M. K., Adewumi, O. O., Oladefedehan, A. O., Awofolaji, A. O., & Adeniji, A. A. (2010).
Effects of residual cyanide in processed cassava peal meals on haematological and biochemical indices of growing rabbits (p.212). Proceedings of 35th Annual Conference of Nigerian Society for Animal Production.
[56]. Isaac, L. J., Abah, G., Akpan, B., & Ekaette, I. U. (2013). Haematological properties of different breeds and sexes of rabbits (p.24-
27). Proceedings of the 18th Annual Conference of Animal Science Association of Nigeria. [57]. Ogunbajo, S. O., Alemede, I. C., Adama, J. Y., & Abdullahi, J. (2009). Haematologicalparameters of Savannah brown does fed
varying dietary levels of flamboyant tree seed meal(p. 88-91). Proceedings of 34th Annual Conference of Nigerian Society for
Animal roduction. [58]. Doyle, D. (2006). William Hewson (1739-74). The father of haematology. British Journal of Haematology, 133(4), 375-381.
[59]. Aderemi, F. A. (2004). Effects of replacement of wheat bran with cassava root sieviatesupplemented or unsupplemented with
enzyme on the haematology and serum biochemistry ofpullet chicks. Tropical Journal of Animal Science, 7, 147-153. [60]. Afolabi, K.D., Akinsoyinu, A.O., Olajide, R. and Akinleye, S.B. (2010). Haematological parameters of the Nigerian local grower
chickens fed varying dietary levels of palm kernel cake. Proceeding of 35th Annual Conference of Nigerian Society for Animal
Prouction (NSAP), Ibadan, Nigeria, 347-349. [61]. Muhammad, A.I., Adamu, S.B., Alade, N.K., Amin, A.B. and Abdulazeez, H. (2015). Studies on haematology and serum
biochemistry of broiler chickens finished on an unprocessed and processed Velvet Bean (Mucona pruriens L.) as dietary protein
source. An International J. of the Nigerian Society for Experimental Biology. Vol. 27(no.2) 68-75. [62]. Muhammad, N. O. and Oloyede, O. B. (2009). Haematological parameters of Broiler chicks fed Aspergillus Niger fermented
Terminalia catappa seed Meal-Based Diet. Global Journal of Biotechnology and Biochemistry 4(2): 179 – 183.
[63]. Tufan, K. and Ramazan, C. (2011). Haematological and biochemical values of the blood of pheasants (Phasianus colchicus) of different ages. Turk. J. Vet. Anim. Sci. 35(3): 149-156
[64]. Palomeque, J., Pinto, D., Viscor, G. (1991). Hematologic and blood chemistry values of the Masai ostrich (Struthio camelus). J.
Wildl. Dis., 27: 34-40. [65]. Cary, N.C. Williams, P.E.V. Geraet, P.A. Uzu, G. and Annison, G. (2002). Factors affecting non-starch polysaccharide digestibility
in poultry. Rhone Poulen. Animal Nutrition, 42 Ar. Aristide Briand BP 10092 164. Antony Cedex, France.
[66]. Adejumo, D.O. (2004). Performance, organ development and haematological indices of rats fed sole diets of graded levels of cassava flour and soybean flour (soygari) as substitutes for energy and protein concentrates. Tropical Journal Animal Science. 7,
57-63
[67]. Oyawoye, E.O. and Ogunkunle, M. (1998). Chemical analysis and biochemical effects of raw jack beans on broiler. Proceeding of
Nigerian Society for Animal Production, 141-142
[68]. Ikhimioya, A., Arijeniwa, I.T. and Ahmed, A. Oleku (2000) Preliminary investigation on the haematology of the Nigerian indigenous chicken. Proceeding of 5th Annual Conference of Animal Science Association of Nigeria, Port Harcourt, 2000, 10-12
[69]. Nebedun, J., Udeafor, P. and Okeke, C. (2010). Comparative effect of ethanolic extracts of Ficus carica and Mucona pruriens leaves
on hematological parameters in albino rats. Biokemistri Vol. 22, No.2. [70]. Okwu, D. E. (2004). Phytochemicals and vitamin content of indigenous species of South Eastern Nigeria. J. Sustain. Agric.
Environ. 6: 30-34.
[71]. Anon, (1980). Guide to the care and use of experimental animals. Vol. 1. Canadian Council on Animal Care. Ottawa, Ontario, Canada. Pp. 85 – 90.
[72]. Mitruka, B. M. & Rawnsley, H. M. (1977). Clinical biochemical and hematological reference values in normal experimental
animals (p.134-135). USA: Masson Publishing Inc. [73]. Tuleun, C.D., Adenkola, A.Y and Oluremi, O.I.A. (2007). Performance characteristics and haematological variables of broiler feed
diet containing mucuna (Mucuna utilis) Seed Meal. Tropical Veterinary. 25: 74 - 81.
[74]. Adenkola, A. Y., Ayo, J. O., Sackey, A. K .B. and Adelaiye, A. B. (2009). Haematology changes in pigs administered with ascorbic acid and transported by road for four hours during the harmattan season. J. Cell Anim. Biol. 3(2):021-028.
[75]. Harper, H., Rodwell, V.M. & Mayes, P.A. (1979). Biokimia. Terjemahan dari: Harper’sBiochemistry. Jakarta: Penerbit
BukuKedokteran EGC. [76]. Ekpenyong, T.E. and Biobaku, W.O. (1986). Growth response of rabbits fed activated sewage sludge and dry poultry waste. Journal
of Applied Rabbit Research. 9(1), 14-16
[77]. Bolu, S.A., H. Aklilu and O.O. Balogun, 2006. Effects of improved locally produced natural vitamin premix on the histology and specific enzyme activities of broilers. Ind. J. Poult. Sci., 6: 223-228.
[78]. Reitman, S. and Frankel, S. (1957). A colorimetric method for the determination of serum glutamic oxalacetic and glutamic pyruvic
transaminases. Am J. Clin Pathol. 28(1):56-63 [79]. Shukla, S.K. and S.P. Parahaurii, 1995. Blood biochemical profiles in induced aflatoxicosis of cockerels. Br. Poult. Sci., 36: 155-
160.
[80]. Wards, N.E., Jones, J. and Maurice, D.V. (1985). In efficiency of proponic acid for depleting laying hens and their progeny of Vitamin B Nutr. Res. Int., 32: 12 1325.
[81]. Eggum, B.O., L. Ynotbek, R.M. Beames, L.L.O. Chuma and S. Weneka, 1982. Influence of diet and Microbial Activities in the
Digestive Tract on Digestibilty. Nitrogen and Energy metabolism in Rats and Pigs. Pot. J. Nutr., pp: 161-165. [82]. Alleyne, G.A.O., F. Viteri and J. Alvarado, 1970. A.M.J in metabolism in man Eds by J.C. Waterlow and J.M.C Stephen. Applied
Science Publisher (1981).
[83]. Johnson F, Giulivi C (2005). "Superoxide dismutases and their impact upon human health". Molecular Aspects of Medicine. 26 (4–5): 340–52.
[84]. Olson, Mark E. Jed, y. and Fahey, W. (2017). Moringa oliefera:a multipurpose tree for the dry topics. Rev. Mex.Biodivers. 82:
1071-1082.
Evaluating the Potentials of Carica papaya seed as phytobiotic to improve feed …
DOI: 10.9790/264X-0601010818 www.iosrjournals.org 18 | Page
[85]. Chelikani, P., Fita, I. and Loewen, P.C. (2004). "Diversity of structures and properties among catalases". Cellular and Molecular
Life Sciences. 61 (2): 192–208.
[86]. Del-Rio, L.A., Sandalio, L.M., Palma, J.M., Bueno, P. and Corpas, F.J. (1992). Metabolism of oxygen radicals in peroxisomes and cellular implications. Free Radical Biology and Medicine 13,557–580.
[87]. Ostrea, E.M., Cepeda, E. E., Fleury, C.A. and Balun, J.E. (1985). "Red Cell Membrane Lipid Peroxidation and Hemolysis
Secondary to Phototherapy". Acta Paediatrica. 74 (3): 378–381. [88]. Kinalski, Sledziewski M, Tejelko A (2000). Lipid peroxidation and scavenging enzyme activity in streptozocin induced diabetes.
Acta Diabetol; 37:179-83.
Umar Muazu, et.al. "Evaluating the Potentials of Carica papaya seed as phytobiotic to improve
feed efficiency, growth performance and serum biochemical prameters in broiler chickens."
IOSR Journal of Biotechnology and Biochemistry (IOSR-JBB), 6(1), (2020): pp. 08-18.